関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 4-(3-Chloropropoxy)-3-methoxyacetophenone | HCID 7314264 | — |
| 反応物 | 3-(4-Piperidinyl)-1,2-benzisoxazole Hydrochloride | HCID 13076437 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | Desfluoro Iloperidone (Impurity) | HCID 10024423 | 47.7% |
反応手順
A mixture of 3-(4-piperidinyl)-1,2-benzisoxazole hydrochloride (4.8 g, 20 mmol), K2CO3 (5.2 g, 40 mmol), 1-[4-(3-chloropropoxy)-3-methoxyphenyl]ethanone (5.3 g, 22 mmol), a few crystals of KI and dimethylformamide (60 ml) was stirred at 90 C. for 16 hours. The reaction was poured into water and the aqueous mixture was extracted with ethyl acetate. The extract was washed (water), dried (MgSO4) and concentrated to afford a brown oil. The oil was chromatographed on a Waters Prep 500 utilizing silica gel columns and ethyl acetate-diethylamine (2%), as eluent. Concentration of the appropriate fractions afforded 3.9 g of product as an off-white solid. Recrystallization from absolute ethyl alcohol afforded 2.6 g (33%) of 1-[4-[3-[4-(1,2-benzisoxazol-3-yl)-1-piperidinyl]propoxy]-3-methoxypehenyl]ethanone, m.p.=102°-104° C., as colorless needles.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05580890 |
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| 出典データセット | uspto-grants-1996_12 |
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| ORD ID | ord-f3f51ac021624790a4fc48a80909b7b1 |
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| 出典メモ | uspto-grants-1996_12 |
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